Pravastatin
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Pravastatin EP Impurity B
| N° de SZ CAT: | SZ-P025003 |
| Número CAS | 722504-46-3 |
| Mol.F. | C23H35O8 : Na |
| Peso Molecular |
439.5 : 23.0 |
| Status de Fatura |
Synthesis on demand |
| Rel. CAS No | 773073-26-0 (free base) |
Nome Químico: Sodium (3R,5R)-3,5-dihydroxy-7-[(1S,2S,6S,8S,8aR)-6-hydroxy-8-[[(2S,3R)3-hydroxy-2-methylbutanoyl]oxy]-2-methyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]heptanoate (as per EP)
Sinônimo: 3′′-(R)-hydroxypravastatin (EP)
Shipping Temperature:
HSN Code: 38229010
Country of Origin: India
Sorrisos: O[C@H]1C[C@H](OC([C@@H](C)[C@H](O)C)=O)[C@@]2([H])C(C=C[C@H](C)[C@@H]2CC[C@H](C[C@@H](O)CC([O-])=O)O)=C1.[Na+]
Pravastatin EP Impurity B is chemically Sodium (3R,5R)-3,5-dihydroxy-7-[(1S,2S,6S,8S,8aR)-6-hydroxy-8-[[(2S,3R)3-hydroxy-2-methylbutanoyl]oxy]-2-methyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]heptanoate (as per EP). It is also known as 3′′-(R)-hydroxypravastatin (EP). Pravastatin EP Impurity B is supplied with detailed characterization data compliant with regulatory guideline. Pravastatin EP Impurity B can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Pravastatin.
The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.
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